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Structure. 2005 Jun;13(6):893-904.

Coupling between catalytic site and collective dynamics: a requirement for mechanochemical activity of enzymes.

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1
Department of Computational Biology, school of Medicine, University of Pittsburgh, Pennsylvania 15261, USA.

Abstract

Growing evidence supports the view that enzymatic activity results from a subtle interplay between chemical kinetics and molecular motions. A systematic analysis is performed here to delineate the type and level of coupling between catalysis and conformational mechanics. The dynamics of a set of 98 enzymes representative of different EC classes are analyzed with the Gaussian network model (GNM) and compared with experimental data. In more than 70% of the examined enzymes, the global hinge centers predicted by the GNM are found to be colocalized with the catalytic sites experimentally identified. Low translational mobility (< 7%) is observed for the catalytic residues, consistent with the fine-tuned design of enzymes to achieve precise mechanochemical activities. Ligand binding sites, while closely neighboring catalytic sites, enjoy a moderate flexibility to accommodate the ligand binding. These findings could serve as additional criteria for assessing drug binding residues and could lessen the computational burden of substrate docking searches.

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PMID:
15939021
PMCID:
PMC1489920
DOI:
10.1016/j.str.2005.03.015
[Indexed for MEDLINE]
Free PMC Article

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